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Geraniol inhibits prostate cancer growth by targeting cell cycle and apoptosis pathways

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dc.contributor.authorKim, Su-Hwa-
dc.contributor.authorBae, Hyun Cheol-
dc.contributor.authorPark, Eun-Jung-
dc.contributor.authorLee, Chae Ryun-
dc.contributor.authorKim, Byung-Joo-
dc.contributor.authorLee, Sanghoon-
dc.contributor.authorPark, Hyun Ho-
dc.contributor.authorKim, Sung-Joon-
dc.contributor.authorSo, Insuk-
dc.contributor.authorKim, Tae Woo-
dc.contributor.authorJeon, Ju-Hong-
dc.date.accessioned2021-09-07T13:25:50Z-
dc.date.available2021-09-07T13:25:50Z-
dc.date.created2021-06-14-
dc.date.issued2011-04-01-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/112678-
dc.description.abstractThe progression of prostate cancer is associated with escape from cell cycle arrest and apoptosis under androgen-depleted conditions. Here, we found that geraniol, a naturally occurring monoterpene, induces cell cycle arrest and apoptosis in cultured cells and tumor grafted mice using PC-3 prostate cancer cells. Geraniol modulated the expression of various cell cycle regulators and Bcl-2 family proteins in PC-3 cells in vitro and in vivo. Furthermore, we showed that the combination of sub-optimal doses of geraniol and docetaxel noticeably suppresses prostate cancer growth in cultured cells and tumor xenograft mice. Therefore, our findings provide insight into unraveling the mechanisms underlying escape from cell cycle arrest and apoptosis and developing therapeutic strategies against prostate cancer. (C) 2011 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectANDROGEN DEPRIVATION THERAPY-
dc.subjectDEPENDENT KINASES-
dc.subjectEXPRESSION-
dc.subjectPROGRESSION-
dc.subjectMODULATORS-
dc.subjectRESISTANCE-
dc.subjectRECEPTOR-
dc.subjectBIOSYNTHESIS-
dc.subjectFLAVOPIRIDOL-
dc.subjectCHEMOTHERAPY-
dc.titleGeraniol inhibits prostate cancer growth by targeting cell cycle and apoptosis pathways-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Tae Woo-
dc.identifier.doi10.1016/j.bbrc.2011.02.124-
dc.identifier.scopusid2-s2.0-79953161349-
dc.identifier.wosid000289541900025-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.407, no.1, pp.129 - 134-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume407-
dc.citation.number1-
dc.citation.startPage129-
dc.citation.endPage134-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusANDROGEN DEPRIVATION THERAPY-
dc.subject.keywordPlusDEPENDENT KINASES-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusMODULATORS-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusBIOSYNTHESIS-
dc.subject.keywordPlusFLAVOPIRIDOL-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordAuthorProstate cancer-
dc.subject.keywordAuthorGeraniol-
dc.subject.keywordAuthorAnticancer activity-
dc.subject.keywordAuthorChemosensitivity-
dc.subject.keywordAuthorCell cycle-
dc.subject.keywordAuthorApoptosis-
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